Canonical Allele Identifier: CA2677313374
Gene: GCM2 HGNC NCBI

Linked Data

gnomAD v4: 6-10877133-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877133T>C , CM000668.2:g.10877133T>C GRCh38
NC_000006.11:g.10877366T>C , CM000668.1:g.10877366T>C GRCh37
NC_000006.10:g.10985352T>C NCBI36
NG_008970.1:g.9733A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.343+7A>G MANE Select ENSP00000368805.4:n.343+7A>G
ENST00000379491.4:c.343+7A>G ENSP00000368805.4:n.343+7A>G
ENST00000480294.1:c.101-14380T>C ENSP00000417929.1:n.101-14380T>C
NM_004752.3:c.343+7A>G NP_004743.1:n.343+7A>G
XM_011514991.1:c.343+7A>G XP_011513293.1:n.343+7A>G
NM_004752.4:c.343+7A>G MANE Select NP_004743.1:n.343+7A>G
Search 100 bp 5'
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