Canonical Allele Identifier: CA11841689
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10520358

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176666743C>T , CM000666.2:g.176666743C>T GRCh38
NC_000004.10:g.177824888C>T NCBI36
NC_000004.11:g.177587894C>T , CM000666.1:g.177587894C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_939498.1:n.121-2878C>T
XR_939499.1:n.121-2878C>T
XR_939498.2:n.208-2878C>T
XR_939499.2:n.204-2878C>T