Canonical Allele Identifier: CA1458424502
Gene:

Linked Data

dbSNP Id: rs1014652808

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072397G>C , CM000666.2:g.54072397G>C GRCh38
NC_000004.11:g.54938564G>C , CM000666.1:g.54938564G>C GRCh37
NC_000004.10:g.54633321G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202528G>C ENSP00000423325.1:n.1018-202528G>C