Canonical Allele Identifier: CA362722660
Gene: GCM2 HGNC NCBI

Linked Data

gnomAD v4: 6-10874351-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874351C>T , CM000668.2:g.10874351C>T GRCh38
NC_000006.11:g.10874584C>T , CM000668.1:g.10874584C>T GRCh37
NC_000006.10:g.10982570C>T NCBI36
NG_008970.1:g.12515G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1165G>A MANE Select ENSP00000368805.4:p.Val389Met
ENST00000379491.4:c.1165G>A ENSP00000368805.4:p.Val389Met
ENST00000480294.1:c.101-17162C>T ENSP00000417929.1:n.101-17162C>T
NM_004752.3:c.1165G>A NP_004743.1:p.Val389Met
XM_011514991.1:c.1165G>A XP_011513293.1:p.Val389Met
NM_004752.4:c.1165G>A MANE Select NP_004743.1:p.Val389Met