Canonical Allele Identifier: CA2470001213
Gene:

Linked Data

dbSNP Id: rs1603117123

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606182T>C , CM000686.2:g.8606182T>C GRCh38
NC_000024.9:g.8474223T>C , CM000686.1:g.8474223T>C GRCh37
NC_000024.8:g.8534223T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624507.1:c.53-1151A>G ENSP00000485522.1:n.53-1151A>G
ENST00000624593.1:c.92+16670A>G ENSP00000485106.1:n.92+16670A>G