Canonical Allele Identifier: CA362724518
Gene: GCM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877141C>G , CM000668.2:g.10877141C>G GRCh38
NC_000006.11:g.10877374C>G , CM000668.1:g.10877374C>G GRCh37
NC_000006.10:g.10985360C>G NCBI36
NG_008970.1:g.9725G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.342G>C MANE Select ENSP00000368805.4:p.Gln114His
ENST00000379491.4:c.342G>C ENSP00000368805.4:p.Gln114His
ENST00000480294.1:c.101-14372C>G ENSP00000417929.1:n.101-14372C>G
NM_004752.3:c.342G>C NP_004743.1:p.Gln114His
XM_011514991.1:c.342G>C XP_011513293.1:p.Gln114His
NM_004752.4:c.342G>C MANE Select NP_004743.1:p.Gln114His