Linked Data
dbSNP Id:
rs778409919
ExAC:
9:94485967 C / G
gnomAD v2:
9-94485967-C-G
gnomAD v4:
9-91723685-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91723685C>G , CM000671.2:g.91723685C>G | GRCh38 |
| NC_000009.11:g.94485967C>G , CM000671.1:g.94485967C>G | GRCh37 |
| NC_000009.10:g.93525788C>G | NCBI36 |
| NG_008089.1:g.231478G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.2809G>C MANE Select | ENSP00000364860.3:p.Ala937Pro | |
| ENST00000375708.3:c.2809G>C | ENSP00000364860.3:p.Ala937Pro | |
| ENST00000375715.5:c.1920+469G>C | ENSP00000364867.1:n.1920+469G>C | |
| ENST00000550066.5:n.3277G>C | ||
| NM_004560.3:c.2809G>C | NP_004551.2:p.Ala937Pro | |
| XM_005252008.3:c.2389G>C | XP_005252065.1:p.Ala797Pro | |
| XM_005252009.3:c.1606G>C | XP_005252066.1:p.Ala536Pro | |
| XM_006717121.2:c.2389G>C | XP_006717184.1:p.Ala797Pro | |
| XM_011518721.1:c.2389G>C | XP_011517023.1:p.Ala797Pro | |
| XM_005252008.4:c.2389G>C | XP_005252065.1:p.Ala797Pro | |
| XM_006717121.3:c.2389G>C | XP_006717184.1:p.Ala797Pro | |
| XM_017014762.1:c.2800G>C | XP_016870251.1:p.Ala934Pro | |
| XM_017014763.1:c.2389G>C | XP_016870252.1:p.Ala797Pro | |
| NM_004560.4:c.2809G>C MANE Select | NP_004551.2:p.Ala937Pro |