Canonical Allele Identifier: CA3633937
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs759712994
gnomAD v2: 6-10874587-T-G
gnomAD v3: 6-10874354-T-G
gnomAD v4: 6-10874354-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874354T>G , CM000668.2:g.10874354T>G GRCh38
NC_000006.11:g.10874587T>G , CM000668.1:g.10874587T>G GRCh37
NC_000006.10:g.10982573T>G NCBI36
NG_008970.1:g.12512A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1162A>C MANE Select ENSP00000368805.4:p.Lys388Gln
ENST00000379491.4:c.1162A>C ENSP00000368805.4:p.Lys388Gln
ENST00000480294.1:c.101-17159T>G ENSP00000417929.1:n.101-17159T>G
NM_004752.3:c.1162A>C NP_004743.1:p.Lys388Gln
XM_011514991.1:c.1162A>C XP_011513293.1:p.Lys388Gln
NM_004752.4:c.1162A>C MANE Select NP_004743.1:p.Lys388Gln