Canonical Allele Identifier: CA440620478
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422419T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501262T>A , CM000666.2:g.102501262T>A GRCh38
NC_000004.11:g.103422419T>A , CM000666.1:g.103422419T>A GRCh37
NC_000004.10:g.103641451T>A NCBI36
NG_050628.1:g.4934T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.630A>T XP_011530769.1:p.Ala210=
NR_136202.1:n.48+1177A>T
Search 100 bp 5'
Search 100 bp 3'