Canonical Allele Identifier: CA2727353624
Gene:

Linked Data

dbSNP Id: rs2137090019

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398641A>G , CM000674.2:g.115398641A>G GRCh38
NC_000012.11:g.115836446A>G , CM000674.1:g.115836446A>G GRCh37
NC_000012.10:g.114320829A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8454T>C
XR_945389.2:n.701+8454T>C