Linked Data
MyVariant Identifiers:
chr3:g.172165958C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.172448168C>A , CM000665.2:g.172448168C>A | GRCh38 |
| NC_000003.11:g.172165958C>A , CM000665.1:g.172165958C>A | GRCh37 |
| NC_000003.10:g.173648652C>A | NCBI36 |
| NG_021159.1:g.5289G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000241256.3:c.246G>T MANE Select | ENSP00000241256.2:p.Leu82= | |
| ENST00000241256.2:c.246G>T | ENSP00000241256.2:p.Leu82= | |
| ENST00000427970.1:c.246G>T | ENSP00000395344.1:p.Leu82= | |
| NM_004122.2:c.246G>T | NP_004113.1:p.Leu82= | |
| NM_198407.2:c.246G>T MANE Select | NP_940799.1:p.Leu82= |