Canonical Allele Identifier: CA1929213318
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762505G= , CM000672.2:g.94762505G= GRCh38
NC_000010.10:g.96522262G= , CM000672.1:g.96522262G= GRCh37
NC_000010.9:g.96512252G= NCBI36
NG_008384.2:g.4800G=
NG_008384.3:g.4825G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12553G= ENSP00000483243.1:n.932-12553G=