Canonical Allele Identifier: CA1168547973
Gene:

Linked Data

dbSNP Id: rs1645067222

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385067A>C , CM000663.2:g.56385067A>C GRCh38
NC_000001.10:g.56850739A>C , CM000663.1:g.56850739A>C GRCh37
NC_000001.9:g.56623327A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641109.1:c.759+93819T>G ENSP00000493138.1:n.759+93819T>G
ENST00000641346.1:c.366+15027T>G
ENST00000641415.1:c.192+98196T>G
ENST00000641494.1:c.378+98196T>G
ENST00000642129.1:c.768+98196T>G