Canonical Allele Identifier: CA448719483
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10877443G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877210G>A , CM000668.2:g.10877210G>A GRCh38
NC_000006.11:g.10877443G>A , CM000668.1:g.10877443G>A GRCh37
NC_000006.10:g.10985429G>A NCBI36
NG_008970.1:g.9656C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.273C>T MANE Select ENSP00000368805.4:p.Cys91=
ENST00000379491.4:c.273C>T ENSP00000368805.4:p.Cys91=
ENST00000480294.1:c.101-14303G>A ENSP00000417929.1:n.101-14303G>A
NM_004752.3:c.273C>T NP_004743.1:p.Cys91=
XM_011514991.1:c.273C>T XP_011513293.1:p.Cys91=
NM_004752.4:c.273C>T MANE Select NP_004743.1:p.Cys91=
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