Canonical Allele Identifier: CA1458504754
Gene:

Linked Data

dbSNP Id: rs1367928429

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228409G>T , CM000666.2:g.54228409G>T GRCh38
NC_000004.11:g.55094576G>T , CM000666.1:g.55094576G>T GRCh37
NC_000004.10:g.54789333G>T NCBI36
NG_009250.1:g.4313G>T , LRG_309:g.4313G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46516G>T ENSP00000423325.1:n.1018-46516G>T