Canonical Allele Identifier: CA440619656
Gene:

Linked Data

dbSNP Id: rs1738961321
MyVariant Identifiers: chr4:g.103422170C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501013C>A , CM000666.2:g.102501013C>A GRCh38
NC_000004.11:g.103422170C>A , CM000666.1:g.103422170C>A GRCh37
NC_000004.10:g.103641202C>A NCBI36
NG_050628.1:g.4685C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+236G>T XP_011530769.1:n.643+236G>T
NR_136202.1:n.48+1426G>T