Canonical Allele Identifier: CA349852522
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs1688305869
gnomAD v3: 2-188996177-C-A
gnomAD v4: 2-188996177-C-A
MyVariant Identifiers: chr2:g.189860903C>A (hg19) chr2:g.188996177C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188996177C>A , CM000664.2:g.188996177C>A GRCh38
NC_000002.11:g.189860903C>A , CM000664.1:g.189860903C>A GRCh37
NC_000002.10:g.189569148C>A NCBI36
NG_007404.1:g.26805C>A , LRG_3:g.26805C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.1562C>A ENSP00000415346.2:p.Pro521His
ENST00000304636.9:c.1661C>A MANE Select ENSP00000304408.4:p.Pro554His
ENST00000304636.7:c.1661C>A ENSP00000304408.3:p.Pro554His
ENST00000317840.9:c.1661C>A ENSP00000315243.6:p.Pro554His
NM_000090.3:c.1661C>A , LRG_3t1:c.1661C>A NP_000081.1:p.Pro554His
NM_000090.4:c.1661C>A MANE Select NP_000081.2:p.Pro554His
Search 100 bp 5'
Search 100 bp 3'