Canonical Allele Identifier: CA448719067
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10874588A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874355A>T , CM000668.2:g.10874355A>T GRCh38
NC_000006.11:g.10874588A>T , CM000668.1:g.10874588A>T GRCh37
NC_000006.10:g.10982574A>T NCBI36
NG_008970.1:g.12511T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1161T>A MANE Select ENSP00000368805.4:p.Thr387=
ENST00000379491.4:c.1161T>A ENSP00000368805.4:p.Thr387=
ENST00000480294.1:c.101-17158A>T ENSP00000417929.1:n.101-17158A>T
NM_004752.3:c.1161T>A NP_004743.1:p.Thr387=
XM_011514991.1:c.1161T>A XP_011513293.1:p.Thr387=
NM_004752.4:c.1161T>A MANE Select NP_004743.1:p.Thr387=