Canonical Allele Identifier: CA500847871
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1598293660
MyVariant Identifiers: chr17:g.48270013G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192652G>T , CM000679.2:g.50192652G>T GRCh38
NC_000017.10:g.48270013G>T , CM000679.1:g.48270013G>T GRCh37
NC_000017.9:g.45625012G>T NCBI36
NG_007400.1:g.13988C>A , LRG_1:g.13988C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1917C>A MANE Select ENSP00000225964.6:p.Ser639=
ENST00000225964.9:c.1917C>A ENSP00000225964.5:p.Ser639=
ENST00000476387.1:n.266C>A
NM_000088.3:c.1917C>A , LRG_1t1:c.1917C>A NP_000079.2:p.Ser639=
XM_005257058.3:c.1917C>A XP_005257115.2:p.Ser639=
XM_005257059.3:c.999C>A XP_005257116.2:p.Ser333=
XM_011524341.1:c.1719C>A XP_011522643.1:p.Ser573=
XM_005257058.4:c.1917C>A XP_005257115.2:p.Ser639=
XM_005257059.4:c.999C>A XP_005257116.2:p.Ser333=
NM_000088.4:c.1917C>A MANE Select NP_000079.2:p.Ser639=