Canonical Allele Identifier: CA1458424409
Gene:

Linked Data

dbSNP Id: rs1717633023

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072300T>C , CM000666.2:g.54072300T>C GRCh38
NC_000004.11:g.54938467T>C , CM000666.1:g.54938467T>C GRCh37
NC_000004.10:g.54633224T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202625T>C ENSP00000423325.1:n.1018-202625T>C