Canonical Allele Identifier: CA13492252
Gene:

Linked Data

dbSNP Id: rs1946519

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164784A>C , CM000673.2:g.112164784A>C GRCh38
NC_000011.9:g.112035507A>C , CM000673.1:g.112035507A>C GRCh37
NC_000011.8:g.111540717A>C NCBI36
NG_028143.1:g.4334T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-5635A>C
ENST00000531744.5:c.315-5635A>C ENSP00000456957.1:n.315-5635A>C
ENST00000532699.1:c.315-5635A>C ENSP00000456434.1:n.315-5635A>C