Canonical Allele Identifier: CA12448999
Gene:

Linked Data

dbSNP Id: rs11155053

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139338875C>T , CM000668.2:g.139338875C>T GRCh38
NC_000006.11:g.139660012C>T , CM000668.1:g.139660012C>T GRCh37
NC_000006.10:g.139701705C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403909.2:n.768C>T