Canonical Allele Identifier: CA440619637
Gene:

Linked Data

dbSNP Id: rs1738960863
MyVariant Identifiers: chr4:g.103422165C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501008C>T , CM000666.2:g.102501008C>T GRCh38
NC_000004.11:g.103422165C>T , CM000666.1:g.103422165C>T GRCh37
NC_000004.10:g.103641197C>T NCBI36
NG_050628.1:g.4680C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+241G>A XP_011530769.1:n.643+241G>A
NR_136202.1:n.48+1431G>A