Canonical Allele Identifier: CA2596243692
Gene:

Linked Data

dbSNP Id: rs1642016209
gnomAD v3: 1-38158502-C-A
gnomAD v4: 1-38158502-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38158502C>A , CM000663.2:g.38158502C>A GRCh38
NC_000001.10:g.38624174C>A , CM000663.1:g.38624174C>A GRCh37
NC_000001.9:g.38396761C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947202.1:n.45-3191C>A
XR_947203.1:n.61+16788C>A
XR_947204.1:n.45-3191C>A
XR_947205.1:n.45-3191C>A
XR_001737984.1:n.45-3191C>A
XR_001737985.1:n.61+16788C>A
XR_001737986.1:n.45-3191C>A
XR_001737987.1:n.45-3191C>A
XR_002958294.1:n.45-3191C>A
XR_947205.2:n.45-3191C>A