Canonical Allele Identifier: CA788486671
Gene:

Linked Data

dbSNP Id: rs1306775106
gnomAD v3: 4-144559899-T-A
gnomAD v4: 4-144559899-T-A
MyVariant Identifiers: chr4:g.145481051T>A (hg19) chr4:g.144559899T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559899T>A , CM000666.2:g.144559899T>A GRCh38
NC_000004.11:g.145481051T>A , CM000666.1:g.145481051T>A GRCh37
NC_000004.10:g.145700501T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143921A>T ENSP00000497507.1:n.328-143921A>T
XR_939272.1:n.178+2085A>T
XR_939273.1:n.178+2085A>T
XR_939272.2:n.522+2085A>T
XR_939273.2:n.522+2085A>T
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