Linked Data
dbSNP Id:
rs1783897441
gnomAD v3:
7-21880809-C-A
gnomAD v4:
7-21880809-C-A
MyVariant Identifiers:
chr7:g.21920427C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21880809C>A , CM000669.2:g.21880809C>A | GRCh38 |
| NC_000007.13:g.21920427C>A , CM000669.1:g.21920427C>A | GRCh37 |
| NC_000007.12:g.21886952C>A | NCBI36 |
| NG_012886.2:g.342595C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.12303C>A MANE Select | ENSP00000475939.1:p.Gly4101= | |
| ENST00000328843.10:c.12324C>A | ENSP00000330671.7:p.Gly4108= | |
| ENST00000409508.7:c.12303C>A | ENSP00000475939.1:p.Gly4101= | |
| ENST00000620169.4:c.12324C>A | ENSP00000481693.1:p.Gly4108= | |
| NM_001277115.1:c.12303C>A | NP_001264044.1:p.Gly4101= | |
| NM_001277115.2:c.12303C>A MANE Select | NP_001264044.1:p.Gly4101= |