Canonical Allele Identifier: CA1610194981
Gene: GCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877209T= , CM000668.2:g.10877209T= GRCh38
NC_000006.11:g.10877442T= , CM000668.1:g.10877442T= GRCh37
NC_000006.10:g.10985428T= NCBI36
NG_008970.1:g.9657A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.274A= MANE Select ENSP00000368805.4:p.Thr92=
ENST00000379491.4:c.274A= ENSP00000368805.4:p.Thr92=
ENST00000480294.1:c.101-14304T= ENSP00000417929.1:n.101-14304T=
NM_004752.3:c.274A= NP_004743.1:p.Thr92=
XM_011514991.1:c.274A= XP_011513293.1:p.Thr92=
NM_004752.4:c.274A= MANE Select NP_004743.1:p.Thr92=