Canonical Allele Identifier: CA601753825
Gene:

Linked Data

dbSNP Id: rs1318248593

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164878T>C , CM000673.2:g.112164878T>C GRCh38
NC_000011.9:g.112035601T>C , CM000673.1:g.112035601T>C GRCh37
NC_000011.8:g.111540811T>C NCBI36
NG_028143.1:g.4240A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-5541T>C
ENST00000531744.5:c.315-5541T>C ENSP00000456957.1:n.315-5541T>C
ENST00000532699.1:c.315-5541T>C ENSP00000456434.1:n.315-5541T>C