Canonical Allele Identifier: CA440620456
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422411G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501254G>C , CM000666.2:g.102501254G>C GRCh38
NC_000004.11:g.103422411G>C , CM000666.1:g.103422411G>C GRCh37
NC_000004.10:g.103641443G>C NCBI36
NG_050628.1:g.4926G>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.638C>G XP_011530769.1:p.Ala213Gly
NR_136202.1:n.48+1185C>G