Canonical Allele Identifier: CA1630057779
Gene: COL21A1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.56346003T= , CM000668.2:g.56346003T= GRCh38
NC_000006.11:g.56210801T= , CM000668.1:g.56210801T= GRCh37
NC_000006.10:g.56318760T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370819.5:c.-39+47968A= ENSP00000359855.1:n.-39+47968A=
XM_011514924.1:c.-39+47968A= XP_011513226.1:n.-39+47968A=
NM_001318752.1:c.-39+47968A= NP_001305681.1:n.-39+47968A=
XM_011514924.2:c.-39+47968A= XP_011513226.1:n.-39+47968A=
NM_001318752.2:c.-39+47968A= NP_001305681.1:n.-39+47968A=
Search 100 bp 5'
Search 100 bp 3'