Canonical Allele Identifier: CA1929213271
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762441T= , CM000672.2:g.94762441T= GRCh38
NC_000010.10:g.96522198T= , CM000672.1:g.96522198T= GRCh37
NC_000010.9:g.96512188T= NCBI36
NG_008384.2:g.4736T=
NG_008384.3:g.4761T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12617T= ENSP00000483243.1:n.932-12617T=