Canonical Allele Identifier: CA2336566035
Gene:

Linked Data

dbSNP Id: rs781837821

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648333C>G , CM000681.2:g.41648333C>G GRCh38
NC_000019.9:g.42152254C>G , CM000681.1:g.42152254C>G GRCh37
NC_000019.8:g.46844094C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3169G>C