Canonical Allele Identifier: CA440620485
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422421C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501264C>A , CM000666.2:g.102501264C>A GRCh38
NC_000004.11:g.103422421C>A , CM000666.1:g.103422421C>A GRCh37
NC_000004.10:g.103641453C>A NCBI36
NG_050628.1:g.4936C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.628G>T XP_011530769.1:p.Ala210Ser
NR_136202.1:n.48+1175G>T