Canonical Allele Identifier: CA2493232081

Gene:

Linked Data

• dbSNP Id: rs1691635683

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.20485676C>T , CM000664.2:g.20485676C>T	GRCh38
NC_000002.11:g.20685437C>T , CM000664.1:g.20685437C>T	GRCh37
NC_000002.10:g.20548918C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_157978.1:n.530+3062G>A