Canonical Allele Identifier: CA185200381
Gene:

Linked Data

dbSNP Id: rs1053974806

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395734A>T , CM000670.2:g.122395734A>T GRCh38
NC_000008.10:g.123407973A>T , CM000670.1:g.123407973A>T GRCh37
NC_000008.9:g.123477154A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3438T>A
XR_928599.3:n.152+3438T>A