Canonical Allele Identifier: CA1322177757
Gene:

Linked Data

dbSNP Id: rs1689617253

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934689C>T , CM000664.2:g.203934689C>T GRCh38
NC_000002.11:g.204799412C>T , CM000664.1:g.204799412C>T GRCh37
NC_000002.10:g.204507657C>T NCBI36
NG_011586.1:g.2910C>T , LRG_65:g.2910C>T

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1419G>A
XR_001739861.1:n.1579G>A
XR_427213.3:n.474+1419G>A