Canonical Allele Identifier: CA2470001209
Gene:

Linked Data

dbSNP Id: rs2015296701

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606099T>A , CM000686.2:g.8606099T>A GRCh38
NC_000024.9:g.8474140T>A , CM000686.1:g.8474140T>A GRCh37
NC_000024.8:g.8534140T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624507.1:c.53-1068A>T ENSP00000485522.1:n.53-1068A>T
ENST00000624593.1:c.92+16753A>T ENSP00000485106.1:n.92+16753A>T