Canonical Allele Identifier: CA1458424389
Gene:

Linked Data

dbSNP Id: rs1717632766

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072279G>T , CM000666.2:g.54072279G>T GRCh38
NC_000004.11:g.54938446G>T , CM000666.1:g.54938446G>T GRCh37
NC_000004.10:g.54633203G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202646G>T ENSP00000423325.1:n.1018-202646G>T