Canonical Allele Identifier: CA1168547970
Gene:

Linked Data

dbSNP Id: rs1645067200

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385054A>G , CM000663.2:g.56385054A>G GRCh38
NC_000001.10:g.56850726A>G , CM000663.1:g.56850726A>G GRCh37
NC_000001.9:g.56623314A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.759+93832T>C ENSP00000493138.1:n.759+93832T>C
ENST00000641346.1:c.366+15040T>C
ENST00000641415.1:c.192+98209T>C
ENST00000641494.1:c.378+98209T>C
ENST00000642129.1:c.768+98209T>C