Canonical Allele Identifier: CA362722239
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10874382G>C (hg19) chr6:g.10874149G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874149G>C , CM000668.2:g.10874149G>C GRCh38
NC_000006.11:g.10874382G>C , CM000668.1:g.10874382G>C GRCh37
NC_000006.10:g.10982368G>C NCBI36
NG_008970.1:g.12717C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1367C>G MANE Select ENSP00000368805.4:p.Ala456Gly
ENST00000379491.4:c.1367C>G ENSP00000368805.4:p.Ala456Gly
ENST00000480294.1:c.101-17364G>C ENSP00000417929.1:n.101-17364G>C
NM_004752.3:c.1367C>G NP_004743.1:p.Ala456Gly
XM_011514991.1:c.1367C>G XP_011513293.1:p.Ala456Gly
NM_004752.4:c.1367C>G MANE Select NP_004743.1:p.Ala456Gly
Search 100 bp 5'
Search 100 bp 3'