Linked Data
dbSNP Id:
rs1442494843
gnomAD v2:
2-44102482-C-A
gnomAD v3:
2-43875343-C-A
gnomAD v4:
2-43875343-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43875343C>A , CM000664.2:g.43875343C>A | GRCh38 |
| NC_000002.11:g.44102482C>A , CM000664.1:g.44102482C>A | GRCh37 |
| NC_000002.10:g.43955986C>A | NCBI36 |
| NG_008884.1:g.41380C>A | |
| NG_008884.2:g.48402C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272286.4:c.1686C>A MANE Select | ENSP00000272286.2:p.Phe562Leu | |
| ENST00000272286.2:c.1686C>A | ENSP00000272286.2:p.Phe562Leu | |
| NM_022437.2:c.1686C>A | NP_071882.1:p.Phe562Leu | |
| XM_005264483.2:c.1683C>A | XP_005264540.1:p.Phe561Leu | |
| XM_011533029.1:c.1698C>A | XP_011531331.1:p.Phe566Leu | |
| XM_011533030.1:c.1695C>A | XP_011531332.1:p.Phe565Leu | |
| XM_011533031.1:c.1470C>A | XP_011531333.1:p.Phe490Leu | |
| XR_939707.1:n.2188C>A | ||
| NM_001357321.1:c.1683C>A | NP_001344250.1:p.Phe561Leu | |
| XM_011533029.2:c.1698C>A | XP_011531331.1:p.Phe566Leu | |
| XM_011533030.2:c.1695C>A | XP_011531332.1:p.Phe565Leu | |
| XR_001738891.1:n.2202C>A | ||
| XR_939707.2:n.2202C>A | ||
| NM_022437.3:c.1686C>A MANE Select | NP_071882.1:p.Phe562Leu | |
| NM_001357321.2:c.1683C>A | NP_001344250.1:p.Phe561Leu |