Canonical Allele Identifier: CA107748842
Gene:

Linked Data

dbSNP Id: rs1040702441
gnomAD v3: 4-144559922-C-A
gnomAD v4: 4-144559922-C-A
MyVariant Identifiers: chr4:g.145481074C>A (hg19) chr4:g.144559922C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559922C>A , CM000666.2:g.144559922C>A GRCh38
NC_000004.11:g.145481074C>A , CM000666.1:g.145481074C>A GRCh37
NC_000004.10:g.145700524C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143944G>T ENSP00000497507.1:n.328-143944G>T
XR_939272.1:n.178+2062G>T
XR_939273.1:n.178+2062G>T
XR_939272.2:n.522+2062G>T
XR_939273.2:n.522+2062G>T
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