Canonical Allele Identifier: CA1630057796
Gene: COL21A1 HGNC NCBI

Linked Data

dbSNP Id: rs1765590320

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.56346047dup , CM000668.2:g.56346047dup GRCh38
NC_000006.11:g.56210845dup , CM000668.1:g.56210845dup GRCh37
NC_000006.10:g.56318804dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370819.5:c.-39+47925dup ENSP00000359855.1:n.-39+47925dup
XM_011514924.1:c.-39+47925dup XP_011513226.1:n.-39+47925dup
NM_001318752.1:c.-39+47925dup NP_001305681.1:n.-39+47925dup
XM_011514924.2:c.-39+47925dup XP_011513226.1:n.-39+47925dup
NM_001318752.2:c.-39+47925dup NP_001305681.1:n.-39+47925dup