Canonical Allele Identifier: CA13624435
Gene:

Linked Data

dbSNP Id: rs2227476

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68255036A>T , CM000674.2:g.68255036A>T GRCh38
NC_000012.11:g.68648816A>T , CM000674.1:g.68648816A>T GRCh37
NC_000012.10:g.66935083A>T NCBI36
NG_060763.1:g.3569T>A

Transcript Alleles

HGVS Amino-acid change
XR_945055.1:n.265-9622A>T
XR_002957418.1:n.281-9622A>T