Canonical Allele Identifier: CA337629178
Gene:

Linked Data

dbSNP Id: rs369092836

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907064A>G , CM000686.2:g.8907064A>G GRCh38
NC_000024.9:g.8775105A>G , CM000686.1:g.8775105A>G GRCh37
NC_000024.8:g.8835105A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.110-30A>G