Canonical Allele Identifier: CA2000589928
Gene:

Linked Data

dbSNP Id: rs1474611996

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164633A>G , CM000673.2:g.112164633A>G GRCh38
NC_000011.9:g.112035356A>G , CM000673.1:g.112035356A>G GRCh37
NC_000011.8:g.111540566A>G NCBI36
NG_028143.1:g.4485T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-5786A>G
ENST00000531744.5:c.315-5786A>G ENSP00000456957.1:n.315-5786A>G
ENST00000532699.1:c.315-5786A>G ENSP00000456434.1:n.315-5786A>G