Canonical Allele Identifier: CA362724674
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10877450T>A (hg19) chr6:g.10877217T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10877217T>A , CM000668.2:g.10877217T>A GRCh38
NC_000006.11:g.10877450T>A , CM000668.1:g.10877450T>A GRCh37
NC_000006.10:g.10985436T>A NCBI36
NG_008970.1:g.9649A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.266A>T MANE Select ENSP00000368805.4:p.Gln89Leu
ENST00000379491.4:c.266A>T ENSP00000368805.4:p.Gln89Leu
ENST00000480294.1:c.101-14296T>A ENSP00000417929.1:n.101-14296T>A
NM_004752.3:c.266A>T NP_004743.1:p.Gln89Leu
XM_011514991.1:c.266A>T XP_011513293.1:p.Gln89Leu
NM_004752.4:c.266A>T MANE Select NP_004743.1:p.Gln89Leu
Search 100 bp 5'
Search 100 bp 3'