Canonical Allele Identifier: CA2677313372
Gene: GCM2 HGNC NCBI

Linked Data

gnomAD v4: 6-10877125-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877125G>T , CM000668.2:g.10877125G>T GRCh38
NC_000006.11:g.10877358G>T , CM000668.1:g.10877358G>T GRCh37
NC_000006.10:g.10985344G>T NCBI36
NG_008970.1:g.9741C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.343+15C>A MANE Select ENSP00000368805.4:n.343+15C>A
ENST00000379491.4:c.343+15C>A ENSP00000368805.4:n.343+15C>A
ENST00000480294.1:c.101-14388G>T ENSP00000417929.1:n.101-14388G>T
NM_004752.3:c.343+15C>A NP_004743.1:n.343+15C>A
XM_011514991.1:c.343+15C>A XP_011513293.1:n.343+15C>A
NM_004752.4:c.343+15C>A MANE Select NP_004743.1:n.343+15C>A
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