Canonical Allele Identifier: CA426798974
Gene: ACTG2 HGNC NCBI

Linked Data

gnomAD v4: 2-73914843-T-A
MyVariant Identifiers: chr2:g.74141970T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73914843T>A , CM000664.2:g.73914843T>A GRCh38
NC_000002.11:g.74141970T>A , CM000664.1:g.74141970T>A GRCh37
NC_000002.10:g.73995478T>A NCBI36
NG_034140.1:g.26878T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000345517.8:c.777T>A MANE Select ENSP00000295137.3:p.Pro259=
ENST00000345517.7:c.777T>A ENSP00000295137.3:p.Pro259=
ENST00000409624.1:c.777T>A ENSP00000386857.1:p.Pro259=
ENST00000409731.7:c.648T>A ENSP00000386929.3:p.Pro216=
ENST00000438902.6:c.*842T>A ENSP00000410706.2:n.*842T>A
NM_001199893.1:c.648T>A NP_001186822.1:p.Pro216=
NM_001615.3:c.777T>A NP_001606.1:p.Pro259=
NM_001199893.2:c.648T>A NP_001186822.1:p.Pro216=
NM_001615.4:c.777T>A MANE Select NP_001606.1:p.Pro259=
Search 100 bp 5'
Search 100 bp 3'