Canonical Allele Identifier: CA362722431
Gene: GCM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874247C>A , CM000668.2:g.10874247C>A GRCh38
NC_000006.11:g.10874480C>A , CM000668.1:g.10874480C>A GRCh37
NC_000006.10:g.10982466C>A NCBI36
NG_008970.1:g.12619G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1269G>T MANE Select ENSP00000368805.4:p.Met423Ile
ENST00000379491.4:c.1269G>T ENSP00000368805.4:p.Met423Ile
ENST00000480294.1:c.101-17266C>A ENSP00000417929.1:n.101-17266C>A
NM_004752.3:c.1269G>T NP_004743.1:p.Met423Ile
XM_011514991.1:c.1269G>T XP_011513293.1:p.Met423Ile
NM_004752.4:c.1269G>T MANE Select NP_004743.1:p.Met423Ile