Canonical Allele Identifier: CA133346518
Gene:

Linked Data

dbSNP Id: rs757041777

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465851G>T , CM000668.2:g.465851G>T GRCh38
NC_000006.11:g.465851G>T , CM000668.1:g.465851G>T GRCh37
NC_000006.10:g.410851G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12126G>T
XR_926365.1:n.2548+12126G>T
XR_001743914.1:n.482-9357G>T