Canonical Allele Identifier: CA2493233601
Gene:

Linked Data

dbSNP Id: rs13021401

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20488758C>G , CM000664.2:g.20488758C>G GRCh38
NC_000002.11:g.20688519C>G , CM000664.1:g.20688519C>G GRCh37
NC_000002.10:g.20552000C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_157978.1:n.510G>C