Canonical Allele Identifier: CA1095883608
Gene:

Linked Data

dbSNP Id: rs1777187864

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633665G>C , CM000668.2:g.151633665G>C GRCh38
NC_000006.11:g.151954800G>C , CM000668.1:g.151954800G>C GRCh37
NC_000006.10:g.151996493G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3683G>C