Canonical Allele Identifier: CA440619642
Gene:

Linked Data

dbSNP Id: rs1738960973
MyVariant Identifiers: chr4:g.103422166C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501009C>G , CM000666.2:g.102501009C>G GRCh38
NC_000004.11:g.103422166C>G , CM000666.1:g.103422166C>G GRCh37
NC_000004.10:g.103641198C>G NCBI36
NG_050628.1:g.4681C>G

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+240G>C XP_011530769.1:n.643+240G>C
NR_136202.1:n.48+1430G>C