Linked Data
MyVariant Identifiers:
chr3:g.172165940G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.172448150G>C , CM000665.2:g.172448150G>C | GRCh38 |
| NC_000003.11:g.172165940G>C , CM000665.1:g.172165940G>C | GRCh37 |
| NC_000003.10:g.173648634G>C | NCBI36 |
| NG_021159.1:g.5307C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000241256.3:c.264C>G MANE Select | ENSP00000241256.2:p.Ser88= | |
| ENST00000241256.2:c.264C>G | ENSP00000241256.2:p.Ser88= | |
| ENST00000427970.1:c.264C>G | ENSP00000395344.1:p.Ser88= | |
| NM_004122.2:c.264C>G | NP_004113.1:p.Ser88= | |
| NM_198407.2:c.264C>G MANE Select | NP_940799.1:p.Ser88= |