Canonical Allele Identifier: CA74805261
Gene:

Linked Data

dbSNP Id: rs917735913
MyVariant Identifiers: chr3:g.53056976G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056976G>C , CM000665.2:g.53056976G>C GRCh38
NC_000003.11:g.53090992G>C , CM000665.1:g.53090992G>C GRCh37
NC_000003.10:g.53066032G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9737C>G
ENST00000607283.5:c.465-13722C>G
ENST00000607495.5:c.447+20712C>G