Canonical Allele Identifier: CA111347660
Gene: HAFML HGNC NCBI

Linked Data

dbSNP Id: rs910960121
MyVariant Identifiers: chr4:g.177587561T>C (hg19) chr4:g.176666410T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176666410T>C , CM000666.2:g.176666410T>C GRCh38
NC_000004.11:g.177587561T>C , CM000666.1:g.177587561T>C GRCh37
NC_000004.10:g.177824555T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939498.1:n.121-3211T>C
XR_939499.1:n.121-3211T>C
XR_939498.2:n.208-3211T>C
XR_939499.2:n.204-3211T>C
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