Canonical Allele Identifier: CA228572266
Gene:

Linked Data

dbSNP Id: rs1055883913

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166744T>C , CM000673.2:g.112166744T>C GRCh38
NC_000011.9:g.112037467T>C , CM000673.1:g.112037467T>C GRCh37
NC_000011.8:g.111542677T>C NCBI36
NG_028143.1:g.2374A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3675T>C
ENST00000531744.5:c.315-3675T>C ENSP00000456957.1:n.315-3675T>C
ENST00000532699.1:c.315-3675T>C ENSP00000456434.1:n.315-3675T>C