Canonical Allele Identifier: CA103381318
Gene:

Linked Data

dbSNP Id: rs184957688
gnomAD v2: 4-106463929-C-T
gnomAD v3: 4-105542772-C-T
gnomAD v4: 4-105542772-C-T
MyVariant Identifiers: chr4:g.106463929C>T (hg19) chr4:g.105542772C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542772C>T , CM000666.2:g.105542772C>T GRCh38
NC_000004.11:g.106463929C>T , CM000666.1:g.106463929C>T GRCh37
NC_000004.10:g.106683378C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-63G>A
XR_939039.1:n.456-63G>A
XR_939040.1:n.296-1296G>A
XR_001741410.1:n.311-63G>A
XR_001741411.1:n.787-63G>A
XR_001741412.1:n.311-63G>A
XR_001741413.1:n.311-63G>A
XR_001741414.1:n.311-63G>A
XR_939038.2:n.311-63G>A
XR_939040.2:n.311-1296G>A
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