Canonical Allele Identifier: CA440618929
Gene:

Linked Data

dbSNP Id: rs1385417249
MyVariant Identifiers: chr4:g.103422066C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500909C>A , CM000666.2:g.102500909C>A GRCh38
NC_000004.11:g.103422066C>A , CM000666.1:g.103422066C>A GRCh37
NC_000004.10:g.103641098C>A NCBI36
NG_050628.1:g.4581C>A

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+340G>T XP_011530769.1:n.643+340G>T
NR_136202.1:n.48+1530G>T