Canonical Allele Identifier: CA440619648
Gene:

Linked Data

dbSNP Id: rs2149087791
MyVariant Identifiers: chr4:g.103422168G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501011G>A , CM000666.2:g.102501011G>A GRCh38
NC_000004.11:g.103422168G>A , CM000666.1:g.103422168G>A GRCh37
NC_000004.10:g.103641200G>A NCBI36
NG_050628.1:g.4683G>A

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+238C>T XP_011530769.1:n.643+238C>T
NR_136202.1:n.48+1428C>T