Canonical Allele Identifier: CA1610190095
Gene: GCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874348A= , CM000668.2:g.10874348A= GRCh38
NC_000006.11:g.10874581A= , CM000668.1:g.10874581A= GRCh37
NC_000006.10:g.10982567A= NCBI36
NG_008970.1:g.12518T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1168T= MANE Select ENSP00000368805.4:p.Ser390=
ENST00000379491.4:c.1168T= ENSP00000368805.4:p.Ser390=
ENST00000480294.1:c.101-17165A= ENSP00000417929.1:n.101-17165A=
NM_004752.3:c.1168T= NP_004743.1:p.Ser390=
XM_011514991.1:c.1168T= XP_011513293.1:p.Ser390=
NM_004752.4:c.1168T= MANE Select NP_004743.1:p.Ser390=