Linked Data
dbSNP Id:
rs782248141
ExAC:
X:154225381 G / T
gnomAD v2:
X-154225381-G-T
gnomAD v4:
X-154997106-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154997106G>T , CM000685.2:g.154997106G>T | GRCh38 |
| NC_000023.10:g.154225381G>T , CM000685.1:g.154225381G>T | GRCh37 |
| NC_000023.9:g.153878575G>T | NCBI36 |
| NG_011403.1:g.30618C>A | |
| NG_011403.2:g.30618C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.266-11C>A MANE Select | ENSP00000353393.4:n.266-11C>A | |
| ENST00000647125.1:c.*52-11C>A | ENSP00000496062.1:n.*52-11C>A | |
| ENST00000360256.8:c.266-11C>A | ENSP00000353393.4:n.266-11C>A | |
| ENST00000423959.5:c.161-11C>A | ENSP00000409446.1:n.161-11C>A | |
| ENST00000453950.1:c.248-11C>A | ENSP00000389153.1:n.248-11C>A | |
| NM_000132.3:c.266-11C>A | NP_000123.1:n.266-11C>A | |
| XM_011531126.1:c.161-11C>A | XP_011529428.1:n.161-11C>A | |
| NM_000132.4:c.266-11C>A MANE Select | NP_000123.1:n.266-11C>A |