Canonical Allele Identifier: CA448719061
Gene: GCM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10874585T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874352T>C , CM000668.2:g.10874352T>C GRCh38
NC_000006.11:g.10874585T>C , CM000668.1:g.10874585T>C GRCh37
NC_000006.10:g.10982571T>C NCBI36
NG_008970.1:g.12514A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1164A>G MANE Select ENSP00000368805.4:p.Lys388=
ENST00000379491.4:c.1164A>G ENSP00000368805.4:p.Lys388=
ENST00000480294.1:c.101-17161T>C ENSP00000417929.1:n.101-17161T>C
NM_004752.3:c.1164A>G NP_004743.1:p.Lys388=
XM_011514991.1:c.1164A>G XP_011513293.1:p.Lys388=
NM_004752.4:c.1164A>G MANE Select NP_004743.1:p.Lys388=
Search 100 bp 5'
Search 100 bp 3'