Canonical Allele Identifier: CA1929213429
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762584G= , CM000672.2:g.94762584G= GRCh38
NC_000010.10:g.96522341G= , CM000672.1:g.96522341G= GRCh37
NC_000010.9:g.96512331G= NCBI36
NG_008384.2:g.4879G=
NG_008384.3:g.4904G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12474G= ENSP00000483243.1:n.932-12474G=