Canonical Allele Identifier: CA362722425
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs1779842720

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874245G>A , CM000668.2:g.10874245G>A GRCh38
NC_000006.11:g.10874478G>A , CM000668.1:g.10874478G>A GRCh37
NC_000006.10:g.10982464G>A NCBI36
NG_008970.1:g.12621C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1271C>T MANE Select ENSP00000368805.4:p.Ser424Phe
ENST00000379491.4:c.1271C>T ENSP00000368805.4:p.Ser424Phe
ENST00000480294.1:c.101-17268G>A ENSP00000417929.1:n.101-17268G>A
NM_004752.3:c.1271C>T NP_004743.1:p.Ser424Phe
XM_011514991.1:c.1271C>T XP_011513293.1:p.Ser424Phe
NM_004752.4:c.1271C>T MANE Select NP_004743.1:p.Ser424Phe