Canonical Allele Identifier: CA400221096
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 983519
ClinVar RCV Id: RCV001263481
dbSNP Id: rs1907549643
MyVariant Identifiers: chr17:g.48273336C>T (hg19) chr17:g.50195975C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195975C>T , CM000679.2:g.50195975C>T GRCh38
NC_000017.10:g.48273336C>T , CM000679.1:g.48273336C>T GRCh37
NC_000017.9:g.45628335C>T NCBI36
NG_007400.1:g.10665G>A , LRG_1:g.10665G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1004G>A MANE Select ENSP00000225964.6:p.Gly335Asp
ENST00000225964.9:c.1004G>A ENSP00000225964.5:p.Gly335Asp
NM_000088.3:c.1004G>A , LRG_1t1:c.1004G>A NP_000079.2:p.Gly335Asp
XM_005257058.3:c.1004G>A XP_005257115.2:p.Gly335Asp
XM_005257059.3:c.957+339G>A XP_005257116.2:n.957+339G>A
XM_011524341.1:c.957+339G>A XP_011522643.1:n.957+339G>A
XM_005257058.4:c.1004G>A XP_005257115.2:p.Gly335Asp
XM_005257059.4:c.957+339G>A XP_005257116.2:n.957+339G>A
NM_000088.4:c.1004G>A MANE Select NP_000079.2:p.Gly335Asp
Search 100 bp 5'
Search 100 bp 3'