Canonical Allele Identifier: CA1005855180
Gene:

Linked Data

dbSNP Id: rs1674963011

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112708242A>C , CM000663.2:g.112708242A>C GRCh38
NC_000001.10:g.113250864A>C , CM000663.1:g.113250864A>C GRCh37
NC_000001.9:g.113052387A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471038.6:n.428+2218T>G
ENST00000605933.5:c.414+2218T>G
ENST00000606505.5:c.414+2218T>G
ENST00000606954.1:c.350+2218T>G
ENST00000607158.5:n.477+2218T>G