Canonical Allele Identifier: CA96311671
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs990292000
gnomAD v3: 4-42962830-A-G
gnomAD v4: 4-42962830-A-G
MyVariant Identifiers: chr4:g.42964847A>G (hg19) chr4:g.42962830A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962830A>G , CM000666.2:g.42962830A>G GRCh38
NC_000004.11:g.42964847A>G , CM000666.1:g.42964847A>G GRCh37
NC_000004.10:g.42659604A>G NCBI36
NG_027718.1:g.74565A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-62A>G MANE Select ENSP00000382670.2:n.385-62A>G
ENST00000399770.2:c.385-62A>G ENSP00000382670.2:n.385-62A>G
NM_001080476.2:c.385-62A>G NP_001073945.1:n.385-62A>G
XM_011513691.1:c.22-62A>G XP_011511993.1:n.22-62A>G
NM_001080476.3:c.385-62A>G MANE Select NP_001073945.1:n.385-62A>G
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