Canonical Allele Identifier: CA228571734

Gene:

Linked Data

• dbSNP Id: rs531230726
• gnomAD v3: 11-112164698-G-A
• gnomAD v4: 11-112164698-G-A
• MyVariant Identifiers: chr11:g.112035421G>A (hg19) ; chr11:g.112164698G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112164698G>A , CM000673.2:g.112164698G>A	GRCh38
NC_000011.9:g.112035421G>A , CM000673.1:g.112035421G>A	GRCh37
NC_000011.8:g.111540631G>A	NCBI36
NG_028143.1:g.4420C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525987.5:n.320-5721G>A
ENST00000531744.5:c.315-5721G>A	ENSP00000456957.1:n.315-5721G>A
ENST00000532699.1:c.315-5721G>A	ENSP00000456434.1:n.315-5721G>A