Canonical Allele Identifier: CA932070371
Gene: COL17A1 HGNC NCBI

Linked Data

dbSNP Id: rs2086322933
gnomAD v3: 10-104038310-C-G
gnomAD v4: 10-104038310-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038310C>G , CM000672.2:g.104038310C>G GRCh38
NC_000010.10:g.105798068C>G , CM000672.1:g.105798068C>G GRCh37
NC_000010.9:g.105788058C>G NCBI36
NG_007069.1:g.52571G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.2935+96G>C ENSP00000358748.3:n.2935+96G>C
ENST00000648076.2:c.3070+96G>C MANE Select ENSP00000497653.1:n.3070+96G>C
ENST00000353479.9:c.3070+96G>C ENSP00000340937.5:n.3070+96G>C
ENST00000369733.7:c.2935+96G>C ENSP00000358748.3:n.2935+96G>C
NM_000494.3:c.3070+96G>C NP_000485.3:n.3070+96G>C
NM_000494.4:c.3070+96G>C MANE Select NP_000485.3:n.3070+96G>C
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