Canonical Allele Identifier: CA554667125
Gene:

Linked Data

dbSNP Id: rs373027835

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601490C>A , CM000666.2:g.134601490C>A GRCh38
NC_000004.11:g.135522645C>A , CM000666.1:g.135522645C>A GRCh37
NC_000004.10:g.135742095C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14131C>A
XR_939214.1:n.392+14131C>A
XR_939214.2:n.392+14131C>A