Canonical Allele Identifier: CA290717935
Gene: HCRT HGNC NCBI

Linked Data

dbSNP Id: rs918382050
gnomAD v3: 17-42184517-G-A
gnomAD v4: 17-42184517-G-A
MyVariant Identifiers: chr17:g.40336535G>A (hg19) chr17:g.42184517G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184517G>A , CM000679.2:g.42184517G>A GRCh38
NC_000017.10:g.40336535G>A , CM000679.1:g.40336535G>A GRCh37
NC_000017.9:g.37590061G>A NCBI36
NG_011448.1:g.5936C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.33C>T MANE Select ENSP00000293330.1:p.Ala11=
NM_001524.1:c.33C>T MANE Select NP_001515.1:p.Ala11=
Search 100 bp 5'
Search 100 bp 3'