Canonical Allele Identifier: CA456490278
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94055330T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426018T>G , CM000669.2:g.94426018T>G GRCh38
NC_000007.13:g.94055330T>G , CM000669.1:g.94055330T>G GRCh37
NC_000007.12:g.93893266T>G NCBI36
NG_007405.1:g.36458T>G , LRG_2:g.36458T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2964T>G MANE Select ENSP00000297268.6:p.Gly988=
ENST00000297268.10:c.2964T>G ENSP00000297268.6:p.Gly988=
ENST00000478215.1:n.523T>G
ENST00000481570.5:n.2937T>G
ENST00000620463.1:c.2958T>G ENSP00000477719.1:p.Gly986=
NM_000089.3:c.2964T>G , LRG_2t1:c.2964T>G NP_000080.2:p.Gly988=
NM_000089.4:c.2964T>G MANE Select NP_000080.2:p.Gly988=
Search 100 bp 5'
Search 100 bp 3'