Canonical Allele Identifier: CA762207695
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs1165051011
MyVariant Identifiers: chr2:g.189872150A>C (hg19) chr2:g.189007424A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189007424A>C , CM000664.2:g.189007424A>C GRCh38
NC_000002.11:g.189872150A>C , CM000664.1:g.189872150A>C GRCh37
NC_000002.10:g.189580395A>C NCBI36
NG_007404.1:g.38052A>C , LRG_3:g.38052A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.3157-76A>C ENSP00000415346.2:n.3157-76A>C
ENST00000304636.9:c.3256-76A>C MANE Select ENSP00000304408.4:n.3256-76A>C
ENST00000304636.7:c.3256-76A>C ENSP00000304408.3:n.3256-76A>C
ENST00000317840.9:c.2528-630A>C ENSP00000315243.6:n.2528-630A>C
NM_000090.3:c.3256-76A>C , LRG_3t1:c.3256-76A>C NP_000081.1:n.3256-76A>C
NM_000090.4:c.3256-76A>C MANE Select NP_000081.2:n.3256-76A>C
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