Canonical Allele Identifier: CA571582789
Gene:

Linked Data

dbSNP Id: rs1389677419

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817519C>T , CM000668.2:g.155817519C>T GRCh38
NC_000006.11:g.156138653C>T , CM000668.1:g.156138653C>T GRCh37
NC_000006.10:g.156180345C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24100C>T
XR_943146.1:n.552-2849G>A
XR_001744423.1:n.606-2849G>A
XR_001744424.1:n.79+24100C>T