Canonical Allele Identifier: CA448719330
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10874477A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874244A>C , CM000668.2:g.10874244A>C GRCh38
NC_000006.11:g.10874477A>C , CM000668.1:g.10874477A>C GRCh37
NC_000006.10:g.10982463A>C NCBI36
NG_008970.1:g.12622T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1272T>G MANE Select ENSP00000368805.4:p.Ser424=
ENST00000379491.4:c.1272T>G ENSP00000368805.4:p.Ser424=
ENST00000480294.1:c.101-17269A>C ENSP00000417929.1:n.101-17269A>C
NM_004752.3:c.1272T>G NP_004743.1:p.Ser424=
XM_011514991.1:c.1272T>G XP_011513293.1:p.Ser424=
NM_004752.4:c.1272T>G MANE Select NP_004743.1:p.Ser424=