Canonical Allele Identifier: CA2000590728
Gene:

Linked Data

dbSNP Id: rs1351836921

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166746C>T , CM000673.2:g.112166746C>T GRCh38
NC_000011.9:g.112037469C>T , CM000673.1:g.112037469C>T GRCh37
NC_000011.8:g.111542679C>T NCBI36
NG_028143.1:g.2372G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3673C>T
ENST00000531744.5:c.315-3673C>T ENSP00000456957.1:n.315-3673C>T
ENST00000532699.1:c.315-3673C>T ENSP00000456434.1:n.315-3673C>T