Canonical Allele Identifier: CA440620334
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422369A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501212A>C , CM000666.2:g.102501212A>C GRCh38
NC_000004.11:g.103422369A>C , CM000666.1:g.103422369A>C GRCh37
NC_000004.10:g.103641401A>C NCBI36
NG_050628.1:g.4884A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+37T>G XP_011530769.1:n.643+37T>G
NR_136202.1:n.48+1227T>G