Canonical Allele Identifier: CA362722434
Gene: GCM2 HGNC NCBI

Linked Data

gnomAD v4: 6-10874248-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874248A>C , CM000668.2:g.10874248A>C GRCh38
NC_000006.11:g.10874481A>C , CM000668.1:g.10874481A>C GRCh37
NC_000006.10:g.10982467A>C NCBI36
NG_008970.1:g.12618T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1268T>G MANE Select ENSP00000368805.4:p.Met423Arg
ENST00000379491.4:c.1268T>G ENSP00000368805.4:p.Met423Arg
ENST00000480294.1:c.101-17265A>C ENSP00000417929.1:n.101-17265A>C
NM_004752.3:c.1268T>G NP_004743.1:p.Met423Arg
XM_011514991.1:c.1268T>G XP_011513293.1:p.Met423Arg
NM_004752.4:c.1268T>G MANE Select NP_004743.1:p.Met423Arg