Canonical Allele Identifier: CA791420628
Gene: HAFML HGNC NCBI

Linked Data

dbSNP Id: rs961407792
MyVariant Identifiers: chr4:g.177587743G>C (hg19) chr4:g.176666592G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176666592G>C , CM000666.2:g.176666592G>C GRCh38
NC_000004.11:g.177587743G>C , CM000666.1:g.177587743G>C GRCh37
NC_000004.10:g.177824737G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939498.1:n.121-3029G>C
XR_939499.1:n.121-3029G>C
XR_939498.2:n.208-3029G>C
XR_939499.2:n.204-3029G>C
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