Canonical Allele Identifier: CA3633912
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs774323324
gnomAD v2: 6-10874471-A-T
gnomAD v4: 6-10874238-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874238A>T , CM000668.2:g.10874238A>T GRCh38
NC_000006.11:g.10874471A>T , CM000668.1:g.10874471A>T GRCh37
NC_000006.10:g.10982457A>T NCBI36
NG_008970.1:g.12628T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1278T>A MANE Select ENSP00000368805.4:p.Tyr426Ter
ENST00000379491.4:c.1278T>A ENSP00000368805.4:p.Tyr426Ter
ENST00000480294.1:c.101-17275A>T ENSP00000417929.1:n.101-17275A>T
NM_004752.3:c.1278T>A NP_004743.1:p.Tyr426Ter
XM_011514991.1:c.1278T>A XP_011513293.1:p.Tyr426Ter
NM_004752.4:c.1278T>A MANE Select NP_004743.1:p.Tyr426Ter