Canonical Allele Identifier: CA228571728

Gene:

Linked Data

• dbSNP Id: rs571351484
• MyVariant Identifiers: chr11:g.112035408A>G (hg19) ; chr11:g.112164685A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112164685A>G , CM000673.2:g.112164685A>G	GRCh38
NC_000011.9:g.112035408A>G , CM000673.1:g.112035408A>G	GRCh37
NC_000011.8:g.111540618A>G	NCBI36
NG_028143.1:g.4433T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525987.5:n.320-5734A>G
ENST00000531744.5:c.315-5734A>G	ENSP00000456957.1:n.315-5734A>G
ENST00000532699.1:c.315-5734A>G	ENSP00000456434.1:n.315-5734A>G