Canonical Allele Identifier: CA2345843987
Gene:

Linked Data

dbSNP Id: rs1775250710

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875470C>G , CM000682.2:g.1875470C>G GRCh38
NC_000020.10:g.1856116C>G , CM000682.1:g.1856116C>G GRCh37
NC_000020.9:g.1804116C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754467.1:n.433-7377G>C