Linked Data
gnomAD v3:
19-40396216-G-T
gnomAD v4:
19-40396216-G-T
MyVariant Identifiers:
chr19:g.40902123G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40396216G>T , CM000681.2:g.40396216G>T | GRCh38 |
| NC_000019.9:g.40902123G>T , CM000681.1:g.40902123G>T | GRCh37 |
| NC_000019.8:g.45593963G>T | NCBI36 |
| NG_007979.1:g.22149C>A , LRG_265:g.22149C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000324001.8:c.2136C>A MANE Select | ENSP00000326018.6:p.Pro712= | |
| ENST00000673881.1:c.1719C>A | ENSP00000501070.1:p.Pro573= | |
| ENST00000674005.2:c.2421C>A | ENSP00000501261.1:p.Pro807= | |
| ENST00000674773.1:c.1719C>A | ENSP00000502579.1:p.Pro573= | |
| ENST00000675517.1:c.2011C>A | ||
| ENST00000676076.1:c.1997C>A | ||
| ENST00000676260.1:c.2098C>A | ||
| ENST00000676316.1:c.2023C>A | ||
| ENST00000291825.11:c.*2341C>A | ENSP00000291825.6:n.*2341C>A | |
| ENST00000324001.7:c.2136C>A | ENSP00000326018.6:p.Pro712= | |
| NM_020956.2:c.*2341C>A , LRG_265t1:c.*2341C>A | NP_066007.1:n.*2341C>A | |
| NM_181882.2:c.2136C>A , LRG_265t2:c.2136C>A | NP_870998.2:p.Pro712= | |
| XM_011527171.1:c.2136C>A | XP_011525473.1:p.Pro712= | |
| XM_011527171.2:c.2136C>A | XP_011525473.1:p.Pro712= | |
| XM_017027046.1:c.2034C>A | XP_016882535.1:p.Pro678= | |
| XM_017027047.1:c.2034C>A | XP_016882536.1:p.Pro678= | |
| NM_181882.3:c.2136C>A MANE Select | NP_870998.2:p.Pro712= |