Canonical Allele Identifier: CA12040384
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs13165747
gnomAD v2: 5-156970151-C-A
gnomAD v3: 5-157543143-C-A
gnomAD v4: 5-157543143-C-A
MyVariant Identifiers: chr5:g.156970151C>A (hg19) chr5:g.157543143C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543143C>A , CM000667.2:g.157543143C>A GRCh38
NC_000005.9:g.156970151C>A , CM000667.1:g.156970151C>A GRCh37
NC_000005.8:g.156902729C>A NCBI36
NG_046960.1:g.37681G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5152G>T MANE Select ENSP00000257527.5:n.252-5152G>T
ENST00000257527.8:c.252-5152G>T ENSP00000257527.4:n.252-5152G>T
ENST00000517905.1:c.252-5152G>T ENSP00000428654.1:n.252-5152G>T
ENST00000517951.5:c.252-5152G>T ENSP00000428376.1:n.252-5152G>T
NM_033274.4:c.252-5152G>T NP_150377.1:n.252-5152G>T
XM_005266003.2:c.252-5152G>T XP_005266060.1:n.252-5152G>T
NM_033274.5:c.252-5152G>T MANE Select NP_150377.1:n.252-5152G>T
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