Canonical Allele Identifier: CA1168547972
Gene:

Linked Data

dbSNP Id: rs1645067212

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385059T>C , CM000663.2:g.56385059T>C GRCh38
NC_000001.10:g.56850731T>C , CM000663.1:g.56850731T>C GRCh37
NC_000001.9:g.56623319T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641109.1:c.759+93827A>G ENSP00000493138.1:n.759+93827A>G
ENST00000641346.1:c.366+15035A>G
ENST00000641415.1:c.192+98204A>G
ENST00000641494.1:c.378+98204A>G
ENST00000642129.1:c.768+98204A>G