Canonical Allele Identifier: CA440620467
Gene:

Linked Data

dbSNP Id: rs946335191
MyVariant Identifiers: chr4:g.103422415C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501258C>A , CM000666.2:g.102501258C>A GRCh38
NC_000004.11:g.103422415C>A , CM000666.1:g.103422415C>A GRCh37
NC_000004.10:g.103641447C>A NCBI36
NG_050628.1:g.4930C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.634G>T XP_011530769.1:p.Gly212Trp
NR_136202.1:n.48+1181G>T