Canonical Allele Identifier: CA430406552
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189873691T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189008965T>C , CM000664.2:g.189008965T>C GRCh38
NC_000002.11:g.189873691T>C , CM000664.1:g.189873691T>C GRCh37
NC_000002.10:g.189581936T>C NCBI36
NG_007404.1:g.39593T>C , LRG_3:g.39593T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.3468T>C ENSP00000415346.2:p.Pro1156=
ENST00000304636.9:c.3567T>C MANE Select ENSP00000304408.4:p.Pro1189=
ENST00000304636.7:c.3567T>C ENSP00000304408.3:p.Pro1189=
ENST00000317840.9:c.2658T>C ENSP00000315243.6:p.Pro886=
ENST00000487010.1:n.664T>C
NM_000090.3:c.3567T>C , LRG_3t1:c.3567T>C NP_000081.1:p.Pro1189=
NM_000090.4:c.3567T>C MANE Select NP_000081.2:p.Pro1189=
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