Canonical Allele Identifier: CA2424866057
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38351716A= , CM000685.2:g.38351716A= GRCh38
NC_000023.10:g.38210969A= , CM000685.1:g.38210969A= GRCh37
NC_000023.9:g.38095913A= NCBI36
NG_008471.1:g.4234A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465127.1:c.172-314405A= ENSP00000417050.1:n.172-314405A=