Canonical Allele Identifier: CA362722670
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs1176511328
gnomAD v4: 6-10874357-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874357T>C , CM000668.2:g.10874357T>C GRCh38
NC_000006.11:g.10874590T>C , CM000668.1:g.10874590T>C GRCh37
NC_000006.10:g.10982576T>C NCBI36
NG_008970.1:g.12509A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1159A>G MANE Select ENSP00000368805.4:p.Thr387Ala
ENST00000379491.4:c.1159A>G ENSP00000368805.4:p.Thr387Ala
ENST00000480294.1:c.101-17156T>C ENSP00000417929.1:n.101-17156T>C
NM_004752.3:c.1159A>G NP_004743.1:p.Thr387Ala
XM_011514991.1:c.1159A>G XP_011513293.1:p.Thr387Ala
NM_004752.4:c.1159A>G MANE Select NP_004743.1:p.Thr387Ala