Linked Data
ClinVar Variation Id:
2296681
ClinVar RCV Id:
RCV004147258
dbSNP Id:
rs1005302617
gnomAD v3:
2-43877816-C-G
gnomAD v4:
2-43877816-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43877816C>G , CM000664.2:g.43877816C>G | GRCh38 |
| NC_000002.11:g.44104955C>G , CM000664.1:g.44104955C>G | GRCh37 |
| NC_000002.10:g.43958459C>G | NCBI36 |
| NG_008884.1:g.43853C>G | |
| NG_008884.2:g.50875C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272286.4:c.1925C>G MANE Select | ENSP00000272286.2:p.Ala642Gly | |
| ENST00000272286.2:c.1925C>G | ENSP00000272286.2:p.Ala642Gly | |
| NM_022437.2:c.1925C>G | NP_071882.1:p.Ala642Gly | |
| XM_005264483.2:c.1922C>G | XP_005264540.1:p.Ala641Gly | |
| XM_011533029.1:c.1937C>G | XP_011531331.1:p.Ala646Gly | |
| XM_011533030.1:c.1934C>G | XP_011531332.1:p.Ala645Gly | |
| XM_011533031.1:c.1709C>G | XP_011531333.1:p.Ala570Gly | |
| XR_939707.1:n.2427C>G | ||
| NM_001357321.1:c.1922C>G | NP_001344250.1:p.Ala641Gly | |
| XM_011533029.2:c.1937C>G | XP_011531331.1:p.Ala646Gly | |
| XM_011533030.2:c.1934C>G | XP_011531332.1:p.Ala645Gly | |
| XR_001738891.1:n.2441C>G | ||
| XR_939707.2:n.2441C>G | ||
| NM_022437.3:c.1925C>G MANE Select | NP_071882.1:p.Ala642Gly | |
| NM_001357321.2:c.1922C>G | NP_001344250.1:p.Ala641Gly |