Canonical Allele Identifier: CA805749799

Gene:

Linked Data

• dbSNP Id: rs1382445883
• MyVariant Identifiers: chr5:g.151734021G>T (hg19) ; chr5:g.152354460G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.152354460G>T , CM000667.2:g.152354460G>T	GRCh38
NC_000005.9:g.151734021G>T , CM000667.1:g.151734021G>T	GRCh37
NC_000005.8:g.151714214G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944433.1:n.196+16597G>T
XR_944433.2:n.197+16597G>T