Canonical Allele Identifier: CA448719041
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10874576G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874343G>A , CM000668.2:g.10874343G>A GRCh38
NC_000006.11:g.10874576G>A , CM000668.1:g.10874576G>A GRCh37
NC_000006.10:g.10982562G>A NCBI36
NG_008970.1:g.12523C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1173C>T MANE Select ENSP00000368805.4:p.Tyr391=
ENST00000379491.4:c.1173C>T ENSP00000368805.4:p.Tyr391=
ENST00000480294.1:c.101-17170G>A ENSP00000417929.1:n.101-17170G>A
NM_004752.3:c.1173C>T NP_004743.1:p.Tyr391=
XM_011514991.1:c.1173C>T XP_011513293.1:p.Tyr391=
NM_004752.4:c.1173C>T MANE Select NP_004743.1:p.Tyr391=