Canonical Allele Identifier: CA362724656
Gene: GCM2 HGNC NCBI

Linked Data

gnomAD v4: 6-10877210-G-C
MyVariant Identifiers: chr6:g.10877443G>C (hg19) chr6:g.10877210G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.273C>G MANE Select ENSP00000368805.4:p.Cys91Trp
ENST00000379491.4:c.273C>G ENSP00000368805.4:p.Cys91Trp
ENST00000480294.1:c.101-14303G>C ENSP00000417929.1:n.101-14303G>C
NM_004752.3:c.273C>G NP_004743.1:p.Cys91Trp
XM_011514991.1:c.273C>G XP_011513293.1:p.Cys91Trp
NM_004752.4:c.273C>G MANE Select NP_004743.1:p.Cys91Trp
Search 100 bp 5'
Search 100 bp 3'