Canonical Allele Identifier: CA1672978995
Gene:

Linked Data

dbSNP Id: rs1582811510

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633436G>C , CM000668.2:g.151633436G>C GRCh38
NC_000006.11:g.151954571G>C , CM000668.1:g.151954571G>C GRCh37
NC_000006.10:g.151996264G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3454G>C