Canonical Allele Identifier: CA421717583
Gene:

Linked Data

MyVariant Identifiers: chr1:g.169073363A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169104125A>C , CM000663.2:g.169104125A>C GRCh38
NC_000001.10:g.169073363A>C , CM000663.1:g.169073363A>C GRCh37
NC_000001.9:g.167339987A>C NCBI36
NG_023230.1:g.2417A>C

Transcript Alleles

HGVS Amino-acid change
XM_011510287.1:c.-1171A>C XP_011508589.1:n.-1171A>C
NR_135799.1:n.2A>C