Canonical Allele Identifier: CA103381299
Gene:

Linked Data

dbSNP Id: rs546413082
gnomAD v3: 4-105542654-T-C
gnomAD v4: 4-105542654-T-C
MyVariant Identifiers: chr4:g.106463811T>C (hg19) chr4:g.105542654T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542654T>C , CM000666.2:g.105542654T>C GRCh38
NC_000004.11:g.106463811T>C , CM000666.1:g.106463811T>C GRCh37
NC_000004.10:g.106683260T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.351A>G
XR_939039.1:n.511A>G
XR_939040.1:n.296-1178A>G
XR_001741410.1:n.366A>G
XR_001741411.1:n.842A>G
XR_001741412.1:n.366A>G
XR_001741413.1:n.366A>G
XR_001741414.1:n.366A>G
XR_939038.2:n.366A>G
XR_939040.2:n.311-1178A>G
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