Canonical Allele Identifier: CA136996230
Gene:

Linked Data

dbSNP Id: rs2040410

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32634921C>T , CM000668.2:g.32634921C>T GRCh38
NC_000006.11:g.32602698C>T , CM000668.1:g.32602698C>T GRCh37
NC_000006.10:g.32710676C>T NCBI36
NG_032876.1:g.2516C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000422863.1:c.-39+2012C>T ENSP00000405797.1:p.=