Canonical Allele Identifier: CA671766298

Gene:

Linked Data

• dbSNP Id: rs1327266892
• MyVariant Identifiers: chr11:g.112035589A>T (hg19) ; chr11:g.112164866A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112164866A>T , CM000673.2:g.112164866A>T	GRCh38
NC_000011.9:g.112035589A>T , CM000673.1:g.112035589A>T	GRCh37
NC_000011.8:g.111540799A>T	NCBI36
NG_028143.1:g.4252T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525987.5:n.320-5553A>T
ENST00000531744.5:c.315-5553A>T	ENSP00000456957.1:n.315-5553A>T
ENST00000532699.1:c.315-5553A>T	ENSP00000456434.1:n.315-5553A>T