Canonical Allele Identifier: CA1610190114
Gene: GCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874354T= , CM000668.2:g.10874354T= GRCh38
NC_000006.11:g.10874587T= , CM000668.1:g.10874587T= GRCh37
NC_000006.10:g.10982573T= NCBI36
NG_008970.1:g.12512A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1162A= MANE Select ENSP00000368805.4:p.Lys388=
ENST00000379491.4:c.1162A= ENSP00000368805.4:p.Lys388=
ENST00000480294.1:c.101-17159T= ENSP00000417929.1:n.101-17159T=
NM_004752.3:c.1162A= NP_004743.1:p.Lys388=
XM_011514991.1:c.1162A= XP_011513293.1:p.Lys388=
NM_004752.4:c.1162A= MANE Select NP_004743.1:p.Lys388=