Linked Data
dbSNP Id:
rs3775442
gnomAD v2:
4-90715231-C-T
gnomAD v3:
4-89794080-C-T
gnomAD v4:
4-89794080-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89794080C>T , CM000666.2:g.89794080C>T | GRCh38 |
| NC_000004.11:g.90715231C>T , CM000666.1:g.90715231C>T | GRCh37 |
| NC_000004.10:g.90934254C>T | NCBI36 |
| NG_011851.1:g.49217G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000394991.8:c.306+28166G>A MANE Select | ENSP00000378442.4:n.306+28166G>A | |
| ENST00000673718.1:c.306+28166G>A | ENSP00000500990.1:n.306+28166G>A | |
| ENST00000673902.1:c.306+28166G>A | ENSP00000501102.1:n.306+28166G>A | |
| ENST00000674129.1:c.306+28166G>A | ENSP00000501269.1:n.306+28166G>A | |
| ENST00000336904.7:c.306+28166G>A | ENSP00000338345.3:n.306+28166G>A | |
| ENST00000345009.8:c.306+28166G>A | ENSP00000343683.4:n.306+28166G>A | |
| ENST00000394986.5:c.306+28166G>A | ENSP00000378437.1:n.306+28166G>A | |
| ENST00000394989.6:c.264+28166G>A | ENSP00000378440.2:n.264+28166G>A | |
| ENST00000394991.7:c.306+28166G>A | ENSP00000378442.3:n.306+28166G>A | |
| ENST00000420646.6:c.306+28166G>A | ENSP00000396241.2:n.306+28166G>A | |
| ENST00000505199.5:c.264+28166G>A | ENSP00000421485.1:n.264+28166G>A | |
| ENST00000506244.5:c.306+28166G>A | ENSP00000422238.1:n.306+28166G>A | |
| ENST00000508895.5:c.306+28166G>A | ENSP00000426955.1:n.306+28166G>A | |
| ENST00000611107.1:c.264+28166G>A | ENSP00000479604.1:n.264+28166G>A | |
| ENST00000618500.4:c.264+28166G>A | ENSP00000484044.1:n.264+28166G>A | |
| NM_000345.3:c.306+28166G>A | NP_000336.1:n.306+28166G>A | |
| NM_001146054.1:c.306+28166G>A | NP_001139526.1:n.306+28166G>A | |
| NM_001146055.1:c.306+28166G>A | NP_001139527.1:n.306+28166G>A | |
| NM_007308.2:c.306+28166G>A | NP_009292.1:n.306+28166G>A | |
| XM_011532203.1:c.307-2415G>A | XP_011530505.1:n.307-2415G>A | |
| XM_011532204.1:c.307-2415G>A | XP_011530506.1:n.307-2415G>A | |
| XM_011532205.1:c.307-2415G>A | XP_011530507.1:n.307-2415G>A | |
| XM_011532206.1:c.307-2415G>A | XP_011530508.1:n.307-2415G>A | |
| XM_011532207.1:c.307-2415G>A | XP_011530509.1:n.307-2415G>A | |
| XM_011532208.1:c.306+28166G>A | XP_011530510.1:n.306+28166G>A | |
| XM_011532204.3:c.307-2415G>A | XP_011530506.1:n.307-2415G>A | |
| XM_011532205.2:c.307-2415G>A | XP_011530507.1:n.307-2415G>A | |
| XM_011532208.2:c.306+28166G>A | XP_011530510.1:n.306+28166G>A | |
| XM_017008562.1:c.306+28166G>A | XP_016864051.1:n.306+28166G>A | |
| XM_017008563.1:c.306+28166G>A | XP_016864052.1:n.306+28166G>A | |
| NM_000345.4:c.306+28166G>A MANE Select | NP_000336.1:n.306+28166G>A | |
| NM_001146054.2:c.306+28166G>A | NP_001139526.1:n.306+28166G>A | |
| NM_001146055.2:c.306+28166G>A | NP_001139527.1:n.306+28166G>A | |
| NM_001375285.1:c.306+28166G>A | NP_001362214.1:n.306+28166G>A | |
| NM_001375286.1:c.306+28166G>A | NP_001362215.1:n.306+28166G>A | |
| NM_001375287.1:c.306+28166G>A | NP_001362216.1:n.306+28166G>A | |
| NM_001375288.1:c.306+28166G>A | NP_001362217.1:n.306+28166G>A | |
| NR_164674.1:n.384+28166G>A | ||
| NR_164675.1:n.531+28166G>A | ||
| NR_164676.1:n.604+28166G>A | ||
| NM_007308.3:c.306+28166G>A | NP_009292.1:n.306+28166G>A |