Canonical Allele Identifier: CA440620241
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422337A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501180A>C , CM000666.2:g.102501180A>C GRCh38
NC_000004.11:g.103422337A>C , CM000666.1:g.103422337A>C GRCh37
NC_000004.10:g.103641369A>C NCBI36
NG_050628.1:g.4852A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+69T>G XP_011530769.1:n.643+69T>G
NR_136202.1:n.48+1259T>G