Canonical Allele Identifier: CA1610194802
Gene: GCM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877127C= , CM000668.2:g.10877127C= GRCh38
NC_000006.11:g.10877360C= , CM000668.1:g.10877360C= GRCh37
NC_000006.10:g.10985346C= NCBI36
NG_008970.1:g.9739G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.343+13G= MANE Select ENSP00000368805.4:n.343+13G=
ENST00000379491.4:c.343+13G= ENSP00000368805.4:n.343+13G=
ENST00000480294.1:c.101-14386C= ENSP00000417929.1:n.101-14386C=
NM_004752.3:c.343+13G= NP_004743.1:n.343+13G=
XM_011514991.1:c.343+13G= XP_011513293.1:n.343+13G=
NM_004752.4:c.343+13G= MANE Select NP_004743.1:n.343+13G=
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