Canonical Allele Identifier: CA2000590781
Gene:

Linked Data

dbSNP Id: rs1866729382

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166883A>G , CM000673.2:g.112166883A>G GRCh38
NC_000011.9:g.112037606A>G , CM000673.1:g.112037606A>G GRCh37
NC_000011.8:g.111542816A>G NCBI36
NG_028143.1:g.2235T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3536A>G
ENST00000531744.5:c.315-3536A>G ENSP00000456957.1:n.315-3536A>G
ENST00000532699.1:c.315-3536A>G ENSP00000456434.1:n.315-3536A>G