Canonical Allele Identifier: CA1610189839
Gene: GCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874245G= , CM000668.2:g.10874245G= GRCh38
NC_000006.11:g.10874478G= , CM000668.1:g.10874478G= GRCh37
NC_000006.10:g.10982464G= NCBI36
NG_008970.1:g.12621C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1271C= MANE Select ENSP00000368805.4:p.Ser424=
ENST00000379491.4:c.1271C= ENSP00000368805.4:p.Ser424=
ENST00000480294.1:c.101-17268G= ENSP00000417929.1:n.101-17268G=
NM_004752.3:c.1271C= NP_004743.1:p.Ser424=
XM_011514991.1:c.1271C= XP_011513293.1:p.Ser424=
NM_004752.4:c.1271C= MANE Select NP_004743.1:p.Ser424=