Canonical Allele Identifier: CA556731640
Gene: HAFML HGNC NCBI

Linked Data

dbSNP Id: rs1262060371
gnomAD v2: 4-177587647-CCACT-C
gnomAD v3: 4-176666496-CCACT-C
gnomAD v4: 4-176666496-CCACT-C
MyVariant Identifiers: chr4:g.177587648_177587651del (hg19) chr4:g.176666497_176666500del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176666499_176666502del , CM000666.2:g.176666499_176666502del GRCh38
NC_000004.11:g.177587650_177587653del , CM000666.1:g.177587650_177587653del GRCh37
NC_000004.10:g.177824644_177824647del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939498.1:n.121-3122_121-3119del
XR_939499.1:n.121-3122_121-3119del
XR_939498.2:n.208-3122_208-3119del
XR_939499.2:n.204-3122_204-3119del
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