Canonical Allele Identifier: CA448719141
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10874372G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874139G>T , CM000668.2:g.10874139G>T GRCh38
NC_000006.11:g.10874372G>T , CM000668.1:g.10874372G>T GRCh37
NC_000006.10:g.10982358G>T NCBI36
NG_008970.1:g.12727C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1377C>A MANE Select ENSP00000368805.4:p.Pro459=
ENST00000379491.4:c.1377C>A ENSP00000368805.4:p.Pro459=
ENST00000480294.1:c.101-17374G>T ENSP00000417929.1:n.101-17374G>T
NM_004752.3:c.1377C>A NP_004743.1:p.Pro459=
XM_011514991.1:c.1377C>A XP_011513293.1:p.Pro459=
NM_004752.4:c.1377C>A MANE Select NP_004743.1:p.Pro459=
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