Canonical Allele Identifier: CA378065556
Gene: COL17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1299565001
gnomAD v2: 10-105793970-G-C
gnomAD v4: 10-104034212-G-C
MyVariant Identifiers: chr10:g.105793970G>C (hg19) chr10:g.104034212G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034212G>C , CM000672.2:g.104034212G>C GRCh38
NC_000010.10:g.105793970G>C , CM000672.1:g.105793970G>C GRCh37
NC_000010.9:g.105783960G>C NCBI36
NG_007069.1:g.56669C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3643C>G ENSP00000358748.3:p.His1215Asp
ENST00000648076.2:c.3889C>G MANE Select ENSP00000497653.1:p.His1297Asp
ENST00000353479.9:c.3889C>G ENSP00000340937.5:p.His1297Asp
ENST00000369733.7:c.3643C>G ENSP00000358748.3:p.His1215Asp
NM_000494.3:c.3889C>G NP_000485.3:p.His1297Asp
NM_000494.4:c.3889C>G MANE Select NP_000485.3:p.His1297Asp
Search 100 bp 5'
Search 100 bp 3'