Canonical Allele Identifier: CA440618900
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422059A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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