Canonical Allele Identifier: CA108745271

Gene:

Linked Data

• dbSNP Id: rs940581096
• MyVariant Identifiers: chr4:g.154864779G>T (hg19) ; chr4:g.153943627G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153943627G>T , CM000666.2:g.153943627G>T	GRCh38
NC_000004.11:g.154864779G>T , CM000666.1:g.154864779G>T	GRCh37
NC_000004.10:g.155084229G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001741892.1:n.1348-5194G>T