Canonical Allele Identifier: CA1672979283
Gene:

Linked Data

dbSNP Id: rs112969974

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633720G>T , CM000668.2:g.151633720G>T GRCh38
NC_000006.11:g.151954855G>T , CM000668.1:g.151954855G>T GRCh37
NC_000006.10:g.151996548G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3738G>T