Canonical Allele Identifier: CA2000590746
Gene:

Linked Data

dbSNP Id: rs1592822757

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166787T>C , CM000673.2:g.112166787T>C GRCh38
NC_000011.9:g.112037510T>C , CM000673.1:g.112037510T>C GRCh37
NC_000011.8:g.111542720T>C NCBI36
NG_028143.1:g.2331A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3632T>C
ENST00000531744.5:c.315-3632T>C ENSP00000456957.1:n.315-3632T>C
ENST00000532699.1:c.315-3632T>C ENSP00000456434.1:n.315-3632T>C