Canonical Allele Identifier: CA2726480769
Gene:

Linked Data

dbSNP Id: rs2120537772

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68248091T>C , CM000674.2:g.68248091T>C GRCh38
NC_000012.11:g.68641871T>C , CM000674.1:g.68641871T>C GRCh37
NC_000012.10:g.66928138T>C NCBI36
NG_060763.1:g.10514A>G

Transcript Alleles

HGVS Amino-acid change
XR_945055.1:n.265-16567T>C
XR_002957418.1:n.281-16567T>C