Canonical Allele Identifier: CA553838313
Gene:

Linked Data

dbSNP Id: rs1446608757
gnomAD v2: 4-106463616-T-A
gnomAD v3: 4-105542459-T-A
gnomAD v4: 4-105542459-T-A
MyVariant Identifiers: chr4:g.106463616T>A (hg19) chr4:g.105542459T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542459T>A , CM000666.2:g.105542459T>A GRCh38
NC_000004.11:g.106463616T>A , CM000666.1:g.106463616T>A GRCh37
NC_000004.10:g.106683065T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.546A>T
XR_939039.1:n.706A>T
XR_939040.1:n.296-983A>T
XR_001741410.1:n.561A>T
XR_001741411.1:n.1037A>T
XR_001741412.1:n.449+112A>T
XR_001741413.1:n.561A>T
XR_001741414.1:n.449+112A>T
XR_939038.2:n.561A>T
XR_939040.2:n.311-983A>T
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