Canonical Allele Identifier: CA2470008829
Gene:

Linked Data

dbSNP Id: rs2015451022

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8734282T>G , CM000686.2:g.8734282T>G GRCh38
NC_000024.9:g.8602323T>G , CM000686.1:g.8602323T>G GRCh37
NC_000024.8:g.8662323T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000623558.1:c.197-5548T>G ENSP00000485446.1:n.197-5548T>G
ENST00000624237.1:c.64-7773T>G ENSP00000485137.1:n.64-7773T>G
ENST00000624593.1:c.-57+14434A>C ENSP00000485106.1:n.-57+14434A>C