Canonical Allele Identifier: CA2727353625
Gene:

Linked Data

dbSNP Id: rs2137090103

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398764C>T , CM000674.2:g.115398764C>T GRCh38
NC_000012.11:g.115836569C>T , CM000674.1:g.115836569C>T GRCh37
NC_000012.10:g.114320952C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8331G>A
XR_945389.2:n.701+8331G>A