Canonical Allele Identifier: CA1929213473
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762616A= , CM000672.2:g.94762616A= GRCh38
NC_000010.10:g.96522373A= , CM000672.1:g.96522373A= GRCh37
NC_000010.9:g.96512363A= NCBI36
NG_008384.2:g.4911A=
NG_008384.3:g.4936A=

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12442A= ENSP00000483243.1:n.932-12442A=