Canonical Allele Identifier: CA1146018574
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112708239T= , CM000663.2:g.112708239T= GRCh38
NC_000001.10:g.113250861T= , CM000663.1:g.113250861T= GRCh37
NC_000001.9:g.113052384T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000471038.6:n.428+2221A=
ENST00000605933.5:c.414+2221A=
ENST00000606505.5:c.414+2221A=
ENST00000606954.1:c.350+2221A=
ENST00000607158.5:n.477+2221A=