Canonical Allele Identifier: CA448719332
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs1561671135
MyVariant Identifiers: chr6:g.10874477A>G (hg19)

Genomic Alleles

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

Transcript Alleles

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