Canonical Allele Identifier: CA440618898
Gene:

Linked Data

dbSNP Id: rs1738950689
MyVariant Identifiers: chr4:g.103422059A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500902A>G , CM000666.2:g.102500902A>G GRCh38
NC_000004.11:g.103422059A>G , CM000666.1:g.103422059A>G GRCh37
NC_000004.10:g.103641091A>G NCBI36
NG_050628.1:g.4574A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+347T>C XP_011530769.1:n.643+347T>C
NR_136202.1:n.48+1537T>C