Canonical Allele Identifier: CA1929213321
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762506A= , CM000672.2:g.94762506A= GRCh38
NC_000010.10:g.96522263A= , CM000672.1:g.96522263A= GRCh37
NC_000010.9:g.96512253A= NCBI36
NG_008384.2:g.4801A=
NG_008384.3:g.4826A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12552A= ENSP00000483243.1:n.932-12552A=