Canonical Allele Identifier: CA1610190120
Gene: GCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874355A= , CM000668.2:g.10874355A= GRCh38
NC_000006.11:g.10874588A= , CM000668.1:g.10874588A= GRCh37
NC_000006.10:g.10982574A= NCBI36
NG_008970.1:g.12511T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1161T= MANE Select ENSP00000368805.4:p.Thr387=
ENST00000379491.4:c.1161T= ENSP00000368805.4:p.Thr387=
ENST00000480294.1:c.101-17158A= ENSP00000417929.1:n.101-17158A=
NM_004752.3:c.1161T= NP_004743.1:p.Thr387=
XM_011514991.1:c.1161T= XP_011513293.1:p.Thr387=
NM_004752.4:c.1161T= MANE Select NP_004743.1:p.Thr387=