Canonical Allele Identifier: CA362722232
Gene: GCM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874146A>C , CM000668.2:g.10874146A>C GRCh38
NC_000006.11:g.10874379A>C , CM000668.1:g.10874379A>C GRCh37
NC_000006.10:g.10982365A>C NCBI36
NG_008970.1:g.12720T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1370T>G MANE Select ENSP00000368805.4:p.Ile457Ser
ENST00000379491.4:c.1370T>G ENSP00000368805.4:p.Ile457Ser
ENST00000480294.1:c.101-17367A>C ENSP00000417929.1:n.101-17367A>C
NM_004752.3:c.1370T>G NP_004743.1:p.Ile457Ser
XM_011514991.1:c.1370T>G XP_011513293.1:p.Ile457Ser
NM_004752.4:c.1370T>G MANE Select NP_004743.1:p.Ile457Ser