Canonical Allele Identifier: CA154409004
Gene:

Linked Data

dbSNP Id: rs549793700
gnomAD v2: 7-13553773-CTCACCAG-C
gnomAD v3: 7-13514148-CTCACCAG-C
gnomAD v4: 7-13514148-CTCACCAG-C
MyVariant Identifiers: chr7:g.13553774_13553780del (hg19) chr7:g.13514149_13514155del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13514151_13514157del , CM000669.2:g.13514151_13514157del GRCh38
NC_000007.13:g.13553776_13553782del , CM000669.1:g.13553776_13553782del GRCh37
NC_000007.12:g.13520301_13520307del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.148-188165_148-188159del
Search 100 bp 5'
Search 100 bp 3'