Canonical Allele Identifier: CA1168547960
Gene:

Linked Data

dbSNP Id: rs546530058

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385033G>C , CM000663.2:g.56385033G>C GRCh38
NC_000001.10:g.56850705G>C , CM000663.1:g.56850705G>C GRCh37
NC_000001.9:g.56623293G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.759+93853C>G ENSP00000493138.1:n.759+93853C>G
ENST00000641346.1:c.366+15061C>G
ENST00000641415.1:c.192+98230C>G
ENST00000641494.1:c.378+98230C>G
ENST00000642129.1:c.768+98230C>G