Canonical Allele Identifier: CA552305351

Gene: ALB

Linked Data

• dbSNP Id: rs1249708135
• gnomAD v2: 4-74275027-T-C
• gnomAD v4: 4-73409310-T-C
• MyVariant Identifiers: chr4:g.74275027T>C (hg19) ; chr4:g.73409310T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409310T>C , CM000666.2:g.73409310T>C	GRCh38
NC_000004.11:g.74275027T>C , CM000666.1:g.74275027T>C	GRCh37
NC_000004.10:g.74493891T>C	NCBI36
NG_009291.1:g.10056T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-45T>C MANE Select	ENSP00000295897.4:n.483-45T>C
ENST00000295897.8:c.483-45T>C	ENSP00000295897.4:n.483-45T>C
ENST00000401494.7:c.138-45T>C	ENSP00000384695.3:n.138-45T>C
ENST00000415165.6:c.138-2686T>C	ENSP00000401820.2:n.138-2686T>C
ENST00000441319.5:c.489-45T>C	ENSP00000392541.1:n.489-45T>C
ENST00000476441.6:c.80-45T>C	ENSP00000423727.1:n.80-45T>C
ENST00000503124.5:c.33-45T>C	ENSP00000421027.1:n.33-45T>C
ENST00000505649.5:n.169-45T>C
ENST00000509063.5:c.483-45T>C	ENSP00000422784.1:n.483-45T>C
ENST00000514786.1:n.452-45T>C
ENST00000621085.4:c.483-45T>C	ENSP00000483421.1:n.483-45T>C
ENST00000621628.4:c.486+234T>C	ENSP00000480485.1:n.486+234T>C
NM_000477.5:c.483-45T>C	NP_000468.1:n.483-45T>C
NM_000477.6:c.483-45T>C	NP_000468.1:n.483-45T>C
NM_000477.7:c.483-45T>C MANE Select	NP_000468.1:n.483-45T>C