Canonical Allele Identifier: CA368219726
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94034194C>G (hg19) chr7:g.94404882C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404882C>G , CM000669.2:g.94404882C>G GRCh38
NC_000007.13:g.94034194C>G , CM000669.1:g.94034194C>G GRCh37
NC_000007.12:g.93872130C>G NCBI36
NG_007405.1:g.15322C>G , LRG_2:g.15322C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.422C>G MANE Select ENSP00000297268.6:p.Ala141Gly
ENST00000297268.10:c.422C>G ENSP00000297268.6:p.Ala141Gly
ENST00000620463.1:c.416C>G ENSP00000477719.1:p.Ala139Gly
NM_000089.3:c.422C>G , LRG_2t1:c.422C>G NP_000080.2:p.Ala141Gly
NM_000089.4:c.422C>G MANE Select NP_000080.2:p.Ala141Gly
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