Linked Data
dbSNP Id:
rs375679562
ExAC:
9:104192137 C / G
gnomAD v2:
9-104192137-C-G
gnomAD v3:
9-101429855-C-G
gnomAD v4:
9-101429855-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101429855C>G , CM000671.2:g.101429855C>G | GRCh38 |
| NC_000009.11:g.104192137C>G , CM000671.1:g.104192137C>G | GRCh37 |
| NC_000009.10:g.103231958C>G | NCBI36 |
| NG_012387.1:g.10926G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647789.2:c.224G>C MANE Select | ENSP00000497767.1:p.Gly75Ala | |
| ENST00000648064.1:c.224G>C | ENSP00000497990.1:p.Gly75Ala | |
| ENST00000648423.1:c.224G>C | ENSP00000497985.1:p.Gly75Ala | |
| ENST00000648758.1:c.224G>C | ENSP00000497731.1:p.Gly75Ala | |
| ENST00000648906.1:n.394G>C | ||
| ENST00000649902.1:c.224G>C | ENSP00000497216.1:p.Gly75Ala | |
| ENST00000650613.1:n.300G>C | ||
| ENST00000374855.8:c.224G>C | ENSP00000363988.4:p.Gly75Ala | |
| ENST00000468981.3:n.21G>C | ||
| ENST00000616752.1:c.224G>C | ENSP00000481363.1:p.Gly75Ala | |
| NM_000035.3:c.224G>C | NP_000026.2:p.Gly75Ala | |
| NM_000035.4:c.224G>C MANE Select | NP_000026.2:p.Gly75Ala |