Canonical Allele Identifier: CA1762609681
Gene:

Linked Data

dbSNP Id: rs1810131108

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9400162G>C , CM000670.2:g.9400162G>C GRCh38
NC_000008.10:g.9257672G>C , CM000670.1:g.9257672G>C GRCh37
NC_000008.9:g.9295082G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948936.1:n.185+3783C>G
XR_948940.1:n.96-3701G>C
XR_948941.1:n.96-13487G>C
XR_002956685.1:n.99-3701G>C
XR_948940.2:n.99-3701G>C
XR_948941.2:n.99-13487G>C