Canonical Allele Identifier: CA456489020
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94415264-T-C
MyVariant Identifiers: chr7:g.94044576T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415264T>C , CM000669.2:g.94415264T>C GRCh38
NC_000007.13:g.94044576T>C , CM000669.1:g.94044576T>C GRCh37
NC_000007.12:g.93882512T>C NCBI36
NG_007405.1:g.25704T>C , LRG_2:g.25704T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1758T>C MANE Select ENSP00000297268.6:p.Gly586=
ENST00000297268.10:c.1758T>C ENSP00000297268.6:p.Gly586=
ENST00000473573.5:n.95T>C
ENST00000488298.5:n.182T>C
ENST00000620463.1:c.1752T>C ENSP00000477719.1:p.Gly584=
NM_000089.3:c.1758T>C , LRG_2t1:c.1758T>C NP_000080.2:p.Gly586=
NM_000089.4:c.1758T>C MANE Select NP_000080.2:p.Gly586=
Search 100 bp 5'
Search 100 bp 3'